先天性多发性关节炎
重症肌无力
自身抗体
关节病
医学
乙酰胆碱受体
胎儿
抗原
肌肉挛缩
免疫学
怀孕
抗体
内分泌学
内科学
受体
生物
解剖
遗传学
作者
Angela Vincent,Claire Newland,David Beeson,Sietske A. Riemersma,John Newsom‐Davis,L. Brueton,Susan Huson
出处
期刊:The Lancet
[Elsevier]
日期:1995-07-01
卷期号:346 (8966): 24-25
被引量:146
标识
DOI:10.1016/s0140-6736(95)92652-6
摘要
Fetal arthrogryposis multiplex congenita (AMC) is characterised by non-progressive multiple joint contractures, which may result in fetal death, and is heterogeneous in origin. It can associate with maternal myasthenia gravis and autoantibodies to muscle acetylcholine receptor (AChR). We found maternal antibodies that selectively inhibit the fetal form of the AChR in a mother who herself had no features of myasthenia gravis. Maternal autoantibodies specific for fetal antigens could be an unrecognised cause of other congenital disorders.
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